AR021716A1 - Inhibidores de transferasa de proteina farnesilo. - Google Patents

Inhibidores de transferasa de proteina farnesilo.

Info

Publication number
AR021716A1
AR021716A1 ARP990106459A ARP990106459A AR021716A1 AR 021716 A1 AR021716 A1 AR 021716A1 AR P990106459 A ARP990106459 A AR P990106459A AR P990106459 A ARP990106459 A AR P990106459A AR 021716 A1 AR021716 A1 AR 021716A1
Authority
AR
Argentina
Prior art keywords
farnesilo
proteina
transfer inhibitors
attached
alkyl group
Prior art date
Application number
ARP990106459A
Other languages
English (en)
Spanish (es)
Original Assignee
Schering Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Schering Corp filed Critical Schering Corp
Publication of AR021716A1 publication Critical patent/AR021716A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
ARP990106459A 1998-12-18 1999-12-16 Inhibidores de transferasa de proteina farnesilo. AR021716A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US21656098A 1998-12-18 1998-12-18

Publications (1)

Publication Number Publication Date
AR021716A1 true AR021716A1 (es) 2002-07-31

Family

ID=22807539

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP990106459A AR021716A1 (es) 1998-12-18 1999-12-16 Inhibidores de transferasa de proteina farnesilo.

Country Status (23)

Country Link
EP (1) EP1140904B1 (enrdf_load_stackoverflow)
JP (1) JP2002533335A (enrdf_load_stackoverflow)
KR (1) KR20010081115A (enrdf_load_stackoverflow)
CN (1) CN1285588C (enrdf_load_stackoverflow)
AR (1) AR021716A1 (enrdf_load_stackoverflow)
AT (1) ATE293622T1 (enrdf_load_stackoverflow)
AU (1) AU2347900A (enrdf_load_stackoverflow)
BR (1) BR9916328A (enrdf_load_stackoverflow)
CA (1) CA2354774C (enrdf_load_stackoverflow)
CO (1) CO5160344A1 (enrdf_load_stackoverflow)
CZ (1) CZ20011900A3 (enrdf_load_stackoverflow)
DE (1) DE69924876T2 (enrdf_load_stackoverflow)
ES (1) ES2237963T3 (enrdf_load_stackoverflow)
HU (1) HUP0203054A3 (enrdf_load_stackoverflow)
ID (1) ID29065A (enrdf_load_stackoverflow)
IL (1) IL143409A0 (enrdf_load_stackoverflow)
NO (1) NO20012960L (enrdf_load_stackoverflow)
PE (1) PE20001516A1 (enrdf_load_stackoverflow)
PL (1) PL348294A1 (enrdf_load_stackoverflow)
SK (1) SK7582001A3 (enrdf_load_stackoverflow)
TR (1) TR200101754T2 (enrdf_load_stackoverflow)
WO (1) WO2000037458A1 (enrdf_load_stackoverflow)
ZA (1) ZA200104236B (enrdf_load_stackoverflow)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1263726B1 (en) * 1999-11-10 2007-09-26 Sanofi-Aventis Deutschland GmbH N-acylpyrrolidin-2-ylalkylbenzamidine derivatives as inhibitors of factor xa
US7361663B2 (en) 1999-11-10 2008-04-22 Aventis Pharmaceuticals Inc. N-acylpyrrolidin-2-ylalkylbenzamidine derivatives as inhibitors of factor Xa
US6589978B2 (en) 2000-06-30 2003-07-08 Hoffman-La Roche Inc. 1-sulfonyl pyrrolidine derivatives
AR033680A1 (es) * 2000-08-30 2004-01-07 Schering Corp Compuestos triciclicos utiles como inhibidores de la farnesil proteino transferasa y su uso para la manufactura de medicamentos como agentes antitumorales
US7342016B2 (en) 2000-08-30 2008-03-11 Schering Corporation Farnesyl protein transferase inhibitors as antitumor agents
US6809093B2 (en) 2000-10-17 2004-10-26 H. Lee Moffitt Cancer & Research Institute, Inc. 2-substituted heterocyclic compounds
US6693099B2 (en) 2000-10-17 2004-02-17 The Procter & Gamble Company Substituted piperazine compounds optionally containing a quinolyl moiety for treating multidrug resistance
US6376514B1 (en) 2000-10-17 2002-04-23 The Procter & Gamble Co. Substituted six-membered heterocyclic compounds useful for treating multidrug resistance and compositions and methods thereof
AU2002236813A1 (en) * 2001-01-22 2002-07-30 Schering Corporation Treatment of malaria with farnesyl protein transferase inhibitors
EP1935887B1 (en) 2001-02-16 2010-01-13 Aventis Pharmaceuticals, Inc. Heterocyclic substituted carbonyl derivatives and their use as dopamine D3 receptor ligands
AU2002257114A1 (en) * 2001-04-06 2002-10-21 Schering Corporation Treatment of malaria with farsenyl protein transferase inhibitors
FR2825705B1 (fr) * 2001-06-08 2005-05-20 Aventis Pharma Sa Nouveaux composes heterocycliques, leur preparation et leur utilisation comme medicaments, notamment comme anti-bacteriens
GB0115862D0 (en) 2001-06-28 2001-08-22 Smithkline Beecham Plc Compounds
US6740757B2 (en) * 2001-08-29 2004-05-25 Pfizer Inc Enantiomers of 6-[(4-chloro-phenyl)-hydroxy-(3-methyl-3h-imidazol-4-yl)-methyl]-4-[3-(3-hydroxy-3-methyl-but-1-ynyl)-phenyl]-1-methyl-1h-quinolin-2-one and salts thereof, useful in the treatment of cancer
FR2835186B1 (fr) 2002-01-28 2006-10-20 Aventis Pharma Sa Nouveaux composes heterocycliques, actifs comme inhibiteurs de beta-lactamases
FR2844273B1 (fr) 2002-09-05 2008-04-04 Aventis Pharma Sa Nouveaux composes heterocycliques, procede et intermediaires de preparation et utilisation comme medicament, notamment comme inhibiteurs de beta-lactamases et anti-bacteriens.
CA2509758A1 (en) * 2002-12-17 2004-07-22 Schering Corporation 17 beta-hydroxysteroid dehydrogenase type 3 inhibitors for the treatment of androgen dependent diseases
JP2008523104A (ja) * 2004-12-13 2008-07-03 シェーリング コーポレイション 癌を治療するための新規なファルネシルタンパク質トランスフェラーゼ阻害剤およびその使用
CN101128202A (zh) 2004-12-14 2008-02-20 先灵公司 法呢基蛋白质转移酶抑制剂和用于治疗增殖性疾病的方法
WO2007084498A1 (en) * 2006-01-19 2007-07-26 Schering Corporation Piperazine derivatives as farnesyl protein transferase inhibitors
CA2724648A1 (en) * 2008-05-22 2009-11-26 Merck Sharp & Dohme Corp. Process for the preparation of an orexin receptor antagonist
HU231150B1 (hu) 2017-03-13 2021-03-29 Richter Gedeon Nyrt Eljárás racém 3-alkilpiperidin-3-karbonsav-etil-észterek optikai izomerjeinek elválasztására
KR20220016918A (ko) 2019-06-04 2022-02-10 하거 바이오사이언시즈, 엘엘씨 오렉신 길항제로서의 이미다졸로 유도체, 조성물 및 방법
TW202220992A (zh) 2020-08-05 2022-06-01 匈牙利商羅特格登公司 具藥理活性之經雜環取代的吡唑并〔1,5-a〕嘧啶衍生物
CN114349711B (zh) * 2022-02-28 2023-08-15 四川依维欣医药科技有限公司 一种(R)-1-Boc-3-羟甲基哌嗪的合成方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL111235A (en) * 1993-10-15 2001-03-19 Schering Plough Corp Medicinal preparations for inhibiting protein G activity and for the treatment of malignant diseases, containing tricyclic compounds, some such new compounds and a process for the preparation of some of them
GB9420172D0 (en) * 1994-10-06 1994-11-23 Boots Co Plc Therapeutic agents
IL117798A (en) * 1995-04-07 2001-11-25 Schering Plough Corp Tricyclic compounds useful for inhibiting the function of protein - G and for the treatment of malignant diseases, and pharmaceutical preparations containing them
HUP0003138A3 (en) * 1997-06-17 2002-11-28 Schering Corp Benzpyrido cycloheptane compounds useful for inhibition of farnesyl protein transferase

Also Published As

Publication number Publication date
ID29065A (id) 2001-07-26
HUP0203054A2 (hu) 2003-01-28
JP2002533335A (ja) 2002-10-08
PE20001516A1 (es) 2001-01-06
HUP0203054A3 (en) 2004-01-28
PL348294A1 (en) 2002-05-20
CZ20011900A3 (cs) 2002-02-13
BR9916328A (pt) 2001-10-02
CN1285588C (zh) 2006-11-22
NO20012960D0 (no) 2001-06-15
CA2354774A1 (en) 2000-06-29
NO20012960L (no) 2001-08-15
KR20010081115A (ko) 2001-08-27
DE69924876T2 (de) 2006-03-02
CN1352642A (zh) 2002-06-05
HK1036279A1 (en) 2001-12-28
EP1140904A1 (en) 2001-10-10
EP1140904B1 (en) 2005-04-20
DE69924876D1 (de) 2005-05-25
WO2000037458A1 (en) 2000-06-29
SK7582001A3 (en) 2002-03-05
TR200101754T2 (tr) 2002-05-21
CO5160344A1 (es) 2002-05-30
ES2237963T3 (es) 2005-08-01
ZA200104236B (en) 2002-08-23
CA2354774C (en) 2009-05-26
ATE293622T1 (de) 2005-05-15
AU2347900A (en) 2000-07-12
IL143409A0 (en) 2002-04-21

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